REGULATORY
Feburic Label to Be Revised due to CV Risk, but No Patient Restrictions to Be Required “at Present”
The Ministry of Health, Labor and Welfare (MHLW) on June 26 presented a number of measures to be taken for the risk of cardiovascular death related to Teijin Pharma’s gout and hyperuricemia treatment Feburic (febuxostat). Measures that limit its use…
To read the full story
Related Article
REGULATORY
- DMD Gene Therapy Elevidys Cleared for NHI Listing at 305 Million Yen
February 13, 2026
- MHLW Orders Label Revisions for Vyxeos, Inlyta, Imbruvica, and More Drugs
February 13, 2026
- MHLW Orders Label Revisions for Sulfite-Containing Medical Products
February 13, 2026
- PMDA Urges Proper Use of Colchicine, Advises against High-Dose Administration
February 12, 2026
- PMDA to Offer Priority Consultations for Overseas Startups
February 12, 2026
The Japanese healthcare sector is experiencing rapid growth, demanding a highly skilled and diverse workforce. However, finding and attracting the best talent in this competitive market presents significant challenges.Enter AI. With the rise of AI-powered tools, healthcare organizations can revolutionize…





